US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 27, 2024 (2 years ago)

Cyanocobalamin Injection, USP, 1,000mcg/mL, 1 mL Multiple-Dose Vial, Rx Only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of particulate matter: glass

What was recalled

Cyanocobalamin Injection, USP, 1,000mcg/mL, 1 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN, 38141, Mfd. in India, NDC 16714-165-01.

Recalling firm
Zydus Pharmaceuticals (USA) Inc
NDC code
16714-165-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0600-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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